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Cleaning Brush with Bristles - Helmut Zepf (85.903.04) - Delynov

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The Brosse de nettoyage soies - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 85.903.04.
  • Reserved for healthcare professionals. Read instructions carefully before use.

17.72 € 17.72 EUR 17.72 € Tax Included

17.72 € Tax Included

(17.72 € / Units)
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Instrument

What is the Helmut Zepf cleaning brush (85.903.04)?

The Helmut Zepf bristle cleaning brush, referenced under code 85.903.04, is a maintenance accessory classified in the category of surgical consumables. This device is specifically developed for the manual processing of reusable medical devices. Manufactured by Helmut Zepf Medizintechnik GmbH, this surgical brush allows reaching complex areas of instruments where debris can accumulate. Its structure is adapted for effective cleaning without altering the surfaces of medical stainless steel tools, thus ensuring optimal preparation before thermal or chemical disinfection and sterilization steps in the practice.

What are the clinical indications for this dental swab?

The use of this dental instrument brush is indicated for the removal of organic soil, such as blood or tissue, after oral surgery, implantology, or periodontology procedures. Manual cleaning is a critical step in the reprocessing of medical devices. This surgical instrument brush allows for the treatment of working parts, hinges, and gripping zones of manual instruments. It is intended exclusively for healthcare professionals who must ensure that each product is perfectly clean and free of visible damage, such as cracks or defects on cutting edges, before any new clinical use.

What are the technical characteristics of the 85.903.04 brush?

The Helmut Zepf cleaning brush is distinguished by its design adapted to the requirements of surgical maintenance. Although delivered non-sterile, it is designed to withstand the repeated cleaning and sterilization cycles inherent to the activity of a dental practice. The manufacturer Helmut Zepf specifies that, due to the product design and the materials used, there is no defined maximum limit for processing cycles, as long as the functional integrity of the brush is preserved. It is imperative to check compatibility with other cleaning products used and to visually inspect the brush for any wear before each use.

What are the contraindications for the use of this device?

The major contraindications mainly concern hypersensitivity reactions. The manufacturer mentions that metal intolerance in the patient can result from indirect or direct contact with the instrument if it is composed of medical stainless steel. If a hypersensitivity reaction is triggered during the procedure, it must be immediately stopped and necessary medical measures must be taken. Furthermore, it is strictly forbidden to use damaged or worn products, presenting breaks or defective edges, as this could compromise patient safety and the effectiveness of dental instrument cleaning.

What precautions should be taken for the maintenance and durability of the product?

Cleaning dental instruments with this brush requires following a strict protocol. All instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The brush itself must undergo rigorous reprocessing. It is crucial to check for the absence of visible damage before each cycle. Due to its non-resorbable nature and its maintenance function, the durability of the brush depends on the frequency of use and compliance with the safety instructions from the manufacturer Helmut Zepf Medizintechnik GmbH. Inadequate maintenance can reduce brushing efficiency and promote the persistence of contaminants on surgical instruments.

Who is the manufacturer and what standards are respected?

The cleaning brush is produced by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I (Class Ir according to certain reprocessing specifications). Compliance with manufacturing standards guarantees the quality of this manual instrument. In accordance with European directives on medical devices, the manufacturer emphasizes that products are delivered non-sterile and must imperatively be cleaned and sterilized before use by qualified healthcare professionals. The use of this equipment falls within a strict regulatory framework aimed at ensuring health safety within dental care facilities.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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